Methane conversion

ABSTRACT

A method for synthesizing hydrocarbons from a methane source which comprises contacting methane with an oxide of germanium at a temperature of 500° to 800° C. The oxide is reduced by the contact and coproduct water is formed. A reducible oxide of germanium is regenerated by oxidizing the reduced composition with molecular oxygen. The oxide GeO 2  is a particularly effective synthesizing agent.

CROSS REFERENCED TO RELATED CASES

This application is a continuation-in-part of U.S. application Ser. No. 412,663, filed Aug. 30, 1982. This application is related to copending, concurrently-filed U.S. patent application Ser. Nos. 522,925; 522,944; 522,942; 522,877; 522,876; 522,906; 522,935; and 522,938, the entire contents of which are incorporated herein by reference.

BACKGROUND OF THE INVENTION

1. Field of the Invention

This invention relates to synthesis of hydrocarbons from a methane source. A particular application of this invention is a method for converting natural gas to more readily transportable material.

2. Description of the Prior Art

A major source of methane is natural gas. Other sources of methane have been considered for fuel supply, e.g., the methane present in coal deposits or formed during mining operations. Relatively small amounts of methane are also produced in various petroleum processes.

The composition of natural gas at the wellhead varies but the major hydrocarbon present is methane. For example the methane content of natural gas may vary within the range of from about 40 to 95 vol. %. Other constituents of natural gas may include ethane, propane, butanes, pentane (and heavier hydrocarbons), hydrogen sulfide, carbon dioxide, helium and nitrogen.

Natural gas is classified as dry or wet depending upon the amount of condensable hydrocarbons contained in it. Condensable hydrocarbons generally comprise C₃ + hydrocarbons although some ethane may be included. Gas conditioning is required to alter the composition of wellhead gas, processing facilities usually being located in or near the production fields. Conventional processing of wellhead natural gas yields processed natural gas containing at least a major amount of methane.

Large-scale use of natural gas often requires a sophisticated and extensive pipeline system. Liquefaction has also been employed as a transportation means, but processes for liquefying, transporting, and revaporizing natural gas are complex, energy-intensive, and require extensive safety precautions. Transport of natural gas has been a continuing problem in the exploitation of natural gas resources. It would be extremely valuable to be able to convert methane (e.g., natural gas) to more easily handleable, or transportable, products. Moreover, direct conversion to olefins such as ethylene or propylene would be extremely valuable to the chemical industry.

In addition to its use as fuel, methane is used for the production of halogenated products (e.g., methyl chloride, methylene chloride, chloroform and carbon tetrachloride). Methane has also been used as a feedstock for producing acetylene by electric-arc or partial-oxidation processes. Electric-arc processes are operated commercially in Europe. In partial-oxidation processes, a feed mixture of oxygen and methane (the methane may contain other, additional hydrocarbons) are preheated to about 540° C. and ignited in a burner. Representative processes of this type are disclosed in U.S. Pat. Nos. 2,679,544; 3,324,300; and 3,244,765. Partial oxidation produces significant quantities of CO, CO₂ and H₂, yielding a dilute acetylene-containing gas and thereby making acetylene recovery difficult.

The largest, non-fuel use of methane is in the production of ammonia and methanol (and formaldehyde). The first, methane conversion, step of these processes is the production of a synthesis gas (CO+H₂) by reforming of methane in the presence of steam over, for example, a nickel catalyst. Typical reformers are tubular furnaces heated with natural gas, the temperatures being maintained at 900° C. and the pressure at about 225 atmospheres.

Pyrolytic or dehydrogenative conversion of methane or natural gas to C₂ + hydrocarbons has previously been proposed. The conversion requires high temperatures (greater than about 1000° C.) and is characterized by the formation of by-product hydrogen. The patent literature contains a number of proposals to catalyze pyrolytic reactions, allowing conversion at lower temperatures. See, for example, U.S. Pat. Nos. 1,656,813; 1,687,890; 1,851,726; 1,863,212; 1,922,918; 1,945,960; 1,958,648; 1,986,238 and 1,988,873. U.S. Pat. No. 2,436,595 discloses and claims a catalytic, dehydrogenative methane-conversion process which employs fluidized beds of heterogeneous catalysts comprising an oxide or other compound of the metals of group VI or VIII.

Including oxygen in a methane feed for conversion over metal oxide catalysts has been proposed. Margolis, L. Ya., Adv. Catal. 14, 429 (1963) and Andtushkevich, T. V., et al, Kinet. Katal. 6, 860 (1965) studied oxygen/methane cofeed over different metal oxides. They report the formation of methanol, formaldehyde, carbon monoxide and carbon dioxide from methane/oxygen feeds. Higher hydrocarbons are either not formed or are converted much faster than methane.

SUMMARY OF THE INVENTION

It has been found that methane may be converted to higher hydrocarbon products by contacting a methane-containing gas with an oxide of germanium at temperatures within the range of about 500° to 800° C. Hydrocarbons produced include lower alkanes, lower olefins, and aromatics. The oxide of germanium is reduced by the methane contact and is easily reoxidazable by contact with an oxygen-containing gas. A preferred oxide of germanium is GeO₂.

The present process is distinguished from previously known pyrolytic methane conversion processes by the use of a reducible oxide of germanium to synthesize higher hydrocarbons from methane with coproduction of water, rather than hydrogen.

The present process is also distinguished from previously suggested methane conversion processes which rely primarily on interactions between methane and at least one of nickel and the noble metals, such as rhodium, palladium, silver, osmium, iridium, platinum and gold. An example of this type of process is disclosed in U.S. Pat. No. 4,205,194. The present process does not require that methane be contacted with one or more of nickel and such noble metals and compounds thereof.

Moreover, in a preferred embodiment, such contacting is carried out in the substantial absence of catalytically effective nickel and the noble metals and compounds thereof to minimize the deleterious catalytic effects of such metals and compounds thereof. For example, at the conditions, e.g., temperatures, useful for the contacting step of the present invention, these metals when contacted with methane tend to promote coke formation, and the metal oxides when contacted with methane tend to promote formation of combustion products (CO_(x)) rather than the desired hydrocarbons. The term "catalytically effective" is used herein to identify that quantity of one or more of nickel and the noble metals and compounds thereof which when present substantially changes the distribution of products obtained in the contacting step of this invention relative to such contacting in the absence of such metals and compounds thereof.

This invention is further described in the following description of its presently preferred embodiments.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a plot of methane conversion to gaseous products and C₂ + hydrocarbon product selectivity vs. time for the combined results of Examples 1 and 2.

FIG. 2 is a plot of methane conversion to gaseous products and C₂ + hydrocarbon product selectivity vs. run time for the results of Example 3.

DETAILED DESCRIPTION OF THE INVENTION

Reducible oxides of germanium can be supplied from a variety of known sources. The term "reducible" is used to identify those oxides of germanium which are reduced by contact with methane at temperatures in the range of 500° to 800° C. Among the reducible oxides of germanium, those containing major amounts of GeO₂ are preferred.

The reducible oxide of germanium is preferably provided as particles. It may be supported by, or diluted with, a conventional support material such as silica, alumina, titania, zirconia, and the like, and combinations thereof. A presently preferred support material is silica.

The term "oxide of germanium" includes: (1) one or more germanium oxides and/or (2) one or more oxygen-containing compounds of manganese, provided that such oxides and compounds have the capability of performing to produce higher hydrocarbon products as set forth herein. The reducible oxides of germanium may be employed alone or in combination with reducible oxides of other metals (see copending U.S. application Ser. Nos. 522,925; 522,944; 522,942; 522,877; 522,876; and 522,906) and/or other oxidative synthesizing agents. Oxidative synthesizing agents are compositions comprising at least one oxide of at least one metal, which composition, when contacted with methane at a temperature selected within the range of about 500° to 1000° C., produces C₂ + hydrocarbon products, coproduct water, and a composition comprising a reduced metal oxide.

Solids may be formed in conventional manner using techniques well known to persons skilled in the art. For example, supported solids may be prepared by conventional methods such as adsorption, impregnation, precipitation, or dry-mixing.

A suitable method is to impregnate the support with solutions of a germanium compound. Some examples of germanium compounds are the acetate, acetylacetonate, oxide, carbide, carbonate, hydroxide, formate, oxalate, nitrate, phosphate, sulfate, sulfide, tartrate, fluoride, chloride, bromide or iodide. Such compounds of germanium may be dissolved in water or other solvent and the solutions are combined with the support and then evaporated to dryness. Preferably, aqueous solutions are employed and water-soluble forms of germanium are used. In some cases, the solutions may have acids and/or bases added to them to facilitate dissolution of the precursors of the oxide of germanium. For example, acids such as hydrochloric or nitric acid or bases such as ammonium hydroxide may be used as desired. The dried solids may then be screened or otherwise processed to form the desired shape, size, or other physical form of the finished solids. Finally, the solids are prepared for use by calcination at high temperatures for a period of time in accordance with conventional practice in this art. For example, the solids are placed in an oven or kiln, or in a tube through which oxygen (e.g., air or oxygen diluted with other gases) is passed, at an elevated temperature (e.g., about 300° to 1200° C., preferably about 500° to 1000° C.).

The foregoing description regarding preparation of solids in a form suitable for the synthesis of hydrocarbons from a methane source is merely illustrative of many possible preparative methods, although it is a particularly suitable method and is preferred.

Germanium loadings on supported solids may be within the range of about 1 to 50 wt. % Ge (calculated as elemental metal).

In addition to methane, the feedstock employed in the method of this invention may contain other hydrocarbon or nonhydrocarbon components, although the methane content should be within the range of about 40 to 100 vol. %, preferably from about 80 to 100 vol. %, more preferably from about 90 to 100 vol %.

Operating temperatures for the contacting of methane-containing gas and a reducible oxide of germanium are in the range of about 500° to 800° C., preferably within the range of about 600° to 750° C.

Operating pressures for the methane contacting step are not critical to the presently claimed invention. However, both general system pressure and the partial pressure of methane have been found to effect overall results. Copending, concurrently filed U.S. application Ser. No. 522,935 discloses a method wherein an oxidative synthesizing agent comprising a reducible metal oxide is contacted with methane, the claimed improvement residing in the use of elevated pressures to promote the formation of C₃ + hydrocarbon products.

Contacting methane and a reducible oxide of germanium to synthesize higher hydrocarbons also produces a reduced oxide of germanium and coproduct water. The exact nature of the reduced form of the synthesizing agent is unknown, and so is referred to herein as "reduced oxide of germanium". Regeneration of a reducible oxide of germanium is readily accomplished by contacting the reduced composition with oxygen (e.g., an oxygen-containing gas such as air) for a period of time sufficient to produce a reducible oxide of germanium from at least a portion of the reduced composition. Oxygen contacting temperatures are preferably within the range of about 300° to 1200° C., more preferably within the range of about 500° to 1000° C.

A single reactor apparatus containing a fixed bed of solids, for example, may be used with intermittent or pulsed flow of a first gas comprising methane and a second gas comprising oxygen (e.g., oxygen, oxygen diluted with an inert gas, or air, preferably air).

Preferably, the methane contacting step and the oxygen contacting step are performed in physically separate zones with solids recirculating between the two zones. Thus, a suitable method for synthesizing hydrocarbons from a methane source comprises: (a) contacting a gas comprising methane and particles comprising a reducible oxide of germanium to form higher hydrocarbon products, coproduct water, and particles comprising a reduced oxide of germanium; (b) removing particles comprising a reduced oxide of germanium from step (a) and contacting the reduced solids with an oxygen-containing gas to form particles comprising a reducible oxide of germanium; and (c) returning particles comprising a reducible oxide of germanium formed in step (b) to step (a). Steps (a), (b) and (c) are preferably repeated at least periodically, and more preferably the steps are continuous. Thus, in this more preferred embodiment, solids are continuously circulated between at least one methane-contact zone and at least one oxygen-contact zone. This more preferred embodiment is disclosed and claimed in copending, concurrently filed U.S. application Ser. No. 522,938.

Particles comprising a reducible oxide of germanium may be contacted with methane in fixed, moving, fluidized, ebullating, or entrained beds of solids. Preferably, methane is contacted with a fluidized bed of particles.

Similarly, particles comprising a reduced oxide of germanium may be contacted with oxygen in fixed, moving, fluidized, ebullating or entrained beds of solids. Preferably, oxygen is contacted with a fluidized bed of particles.

The invention is further illustrated by reference to the following examples.

Experimental results reported below include conversions and selectivities calculated on a molar basis.

EXAMPLE 1

Germanium dioxide (0.36 gram) was dissolved in 100 ml. water over a period of 12 hours. This solution was added to 9.5 grams of Houdry HSC 534 silica and allowed to stand for 1 hour. The mixture was slowly taken to dryness with gentle warming, followed by heating at 110° C. in a drying oven for 2 hours. The dried solid was then further heated to 700° C. at a rate of 2°/minute and held at 700° C. for 10 hours to give a product containing 2.5 weight % germanium. The entire procedure was then repeated using the solid containing 2.5 weight % germanium instead of fresh silica, to give a final germanium oxide/silica solid containing 5 weight % germanium. The finished solid (2.6 grams) was charged to a quartz tube of 0.5 inch inside diameter surrounded by a tubular furnace. The reactor temperature was raised to 700° C. under flowing nitrogen. Nitrogen flow was stopped and methane was introduced into the reactor at a rate of 100 ml./min. (860 hrs.⁻¹ GHSV). The reactor effluent was sampled at the reactor exit and analyzed on a gas chromatograph at a number of time intervals. In addition, all reactor effluent was collected in a sample bag for subsequent analysis of the cumulative reaction products. Results (obtained at about atmospheric pressure and 700° C.) are shown in Table I below. The total amount of carbon oxides formed during reoxidation of the solids (see Example 2, infra) was used to calculate the yield of coke (or other carbonaceous deposit) formed on the solid during the methane run. The instantaneous results shown in Table I are methane conversion to gaseous products and selectivity to these products (i.e., % of C converted to gas phase products). The cumulative results shown in Table I include solid formation.

                  TABLE I                                                          ______________________________________                                         Run   %        % Selectivity*                                                  Time  Conver-                        Ben-                                      (min.)                                                                               sion     C.sub.2 H.sub.4                                                                       C.sub.2 H.sub.6                                                                     C.sub.3                                                                             C.sub.4,5                                                                           zene CO   Coke*                           ______________________________________                                         Instantaneous Results                                                           1    0.39     10.4   26.0 1.0  0.3  0.0  62.3                                  3    0.18     41.3   49.6 5.8  2.5  0.8  0.0                                  10    0.15     53.3   33.3 6.7  4.7  2.0  0.0                                  30    0.13     54.2   27.2 11.4 5.4  1.8  0.0                                  Cumulative Results                                                             30    0.22     31.9   25.2 6.4  3.2  1.4  6.0  25.9                            ______________________________________                                          *Basis of instantaneous results is C converted to gas phase products and       does not include conversion to solid, carbonaceous deposits.             

EXAMPLE 2

After completion of the run described in Example 1, the reactor was flushed with nitrogen for 30 minutes and the solid was reoxidized under flowing air at 700° C. for 90 minutes. The reoxidized solid was then contacted with methane as described in Example 1. Results, shown in Table II below, are presented in the same manner as described in Example 1. FIG. 1 is a plot of methane conversion to gaseous products and C₂ + hydrocarbon selectivity (basis: methane conversion to gaseous products) vs. run time for the combined results of Examples 1 and 2. PG,14

                  TABLE II                                                         ______________________________________                                         Run   %        % Selectivity*                                                  Time  Conver-                        Ben-                                      (min.)                                                                               sion     C.sub.2 H.sub.4                                                                       C.sub.2 H.sub.6                                                                     C.sub.3                                                                             C.sub.4,5                                                                           zene CO   Coke*                           ______________________________________                                         Instantaneous Results                                                           1    0.30     6.8    20.5 0.7  0.3  0.0  71.7                                  3    0.19     37.6   52.6 5.3  3.0  1.5  0.0                                  10    0.17     51.3   32.1 9.0  5.1  2.5  0.0                                  30    0.14     56.4   24.0 12.0 5.4  2.2  0.0                                  Cumulative Results                                                             30    0.21     34.1   21.0 6.8  3.4  1.3  8.4  25.0                            ______________________________________                                          *Basis of instantaneous results is C converted to gas phase products and       does not include conversion to solid, carbonaceous deposits.             

EXAMPLE 3

The procedure of Example 1 was repeated except that the methane run temperature was increased to 750° C. Results are shown in Table III below. FIG. 2 shows the time dependence of methane conversion to all gaseous products and to gaseous hydrocarbons.

                  TABLE III                                                        ______________________________________                                         Run   %        % Selectivity*                                                  Time  Conver-                        Ben-                                      (min.)                                                                               sion     C.sub.2 H.sub.4                                                                       C.sub.2 H.sub.6                                                                     C.sub.3                                                                             C.sub.4,5                                                                           zene CO   Coke*                           ______________________________________                                         Instantaneous Results                                                           1    1.41     38.6   24.6 3.5  2.5  1.9  28.9                                  3    1.14     52.4   11.3 5.0  3.0  5.0  23.3                                 10    0.96     67.5   10.4 6.6  4.2  7.2  4.1                                  30    0.32     66.7   22.5 6.7  2.2  1.9  0.0                                  Cumulative Results                                                             30    1.06     41.1   9.5  4.4  2.3  3.3  8.7  30.7                            ______________________________________                                          *Basis of instantaneous results is C converted to gas phase products and       does not include conversion to solid, carbonaceous deposits.              

What is claimed is:
 1. A method for converting methane to higher hydrocarbon products which comprises contacting a gas comprising methane and a reducible oxide of germanium at a temperature within the range of about 500° to 800° C.
 2. The method of claim 1 wherein the solid is contacted with a gas comprising methane at a temperature within the range of about 600° to 750° C.
 3. The method of claim 1 wherein the gas contains about 40 to 100 vol. % methane.
 4. The method of claim 3 wherein the gas contains about 80 to 100 vol. % methane.
 5. The method of claim 4 wherein the gas contains about 90 to 100 vol. % methane.
 6. The method of claim 1 wherein the gas comprising methane is natural gas.
 7. The method of claim 1 wherein the gas comprising methane is processed natural gas.
 8. The method of claim 1 wherein a gas consisting essentially of methane is contacted with the said reducible oxide.
 9. The method of claim 1 wherein the reducible oxide of germanium comprises GeO₂.
 10. The method of claim 1 wherein the oxide of germanium is associated with a support material.
 11. The method of claim 9 wherein the oxide of germanium is associated with a support material.
 12. The method of claim 10 wherein the support material is silica.
 13. The method of claim 11 wherein the support material is silica.
 14. A method for synthesizing hydrocarbons from a methane source which comprises:(a) contacting a gas comprising methane with a solid comprising a reducible oxide of germanium at a temperature within the range of about 500° C. to 800° C. to form C₂ + hydrocarbons, coproduct water, and solids comprising a reduced oxide of germanium; (b) recovering C₂ + hydrocarbons; (c) at least periodically contacting the solids comprising a reduced oxide of germanium with an oxygen containing gas to produce a solid comprising a reducible oxide of germanium; and (d) contacting a gas comprising methane with the solids product in step (c) as recited in step (a).
 15. The method of claim 14 wherein the temperature of step (c) is within the range of about 300° to 1200° C.
 16. The method of claim 14 wherein the temperature of step (c) is within the range of about 500° to 1000° C.
 17. The method of claim 16 wherein the reducible oxide of germanium comprises GeO₂.
 18. The method of claim 17 wherein the said solid of step (a) comprises GeO₂ on a silica support.
 19. The method of claim 14 wherein solids of step (a) are maintained in the methane-contacting zone as a fluidized bed.
 20. The method of claim 19 wherein solids of step (c) are maintained in the oxygen-contacting zone as a fluidized bed.
 21. The method of claim 20 wherein the temperature of step (a) is within the range of about 600° to 750° C.
 22. The method of claim 21 wherein the temperature of step (c) is within the range of about 500° to 1000° C. 